4-hydroxybutyric acid has been researched along with Child Development Deviations in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 5 (62.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ding, Y; Huang, S; Li, M; Li, X; Liu, Y; Qin, Y; Song, J; Wang, Q; Yang, Y; Zhang, Y | 1 |
| Barker, PB; Lin, DD; Wang, KY | 1 |
| Gibson, KM; Jansen, EE; Pearl, PL; Roullet, JB; Salomons, GS; Vogel, KR | 1 |
| Blasi, P; Crutchfield, SR; Di Rosa, G; Dionisi-Vici, C; Gibson, KM; Malaspina, P; Rizzo, C; Tortorella, G | 1 |
| Gibson, KM; Jakobs, C; Jansen, EE; Mulder, MF; Roos, B; Wamelink, MM | 1 |
| Gibson, KM; Jakobs, C; Jensen, K; Kim, KJ; Malaspina, P; Pearl, PL; Snead, OC | 1 |
| Ergezinger, K; Frauendienst-Egger, G; Gibson, KM; Jeschke, R; Korall, H; Schuster, VH | 1 |
| Bennett, MJ; Ganesh, J; Gibson, KM; Jakobs, C; Knerr, I; Myers, SM; Salomons, GS | 1 |
2 review(s) available for 4-hydroxybutyric acid and Child Development Deviations
| Article | Year |
|---|---|
A case of acute onset succinic semialdehyde dehydrogenase deficiency: neuroimaging findings and literature review.
Topics: Amino Acid Metabolism, Inborn Errors; Developmental Disabilities; Female; Humans; Hydroxybutyrates; Infant; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Succinate-Semialdehyde Dehydrogenase | 2016 |
Succinic semialdehyde dehydrogenase: biochemical-molecular-clinical disease mechanisms, redox regulation, and functional significance.
Topics: Aldehydes; Amino Acid Metabolism, Inborn Errors; Animals; Catalytic Domain; Developmental Disabilities; Disease Models, Animal; gamma-Aminobutyric Acid; Humans; Hydroxybutyrates; Mice; Oxidation-Reduction; Succinate-Semialdehyde Dehydrogenase | 2011 |
6 other study(ies) available for 4-hydroxybutyric acid and Child Development Deviations
| Article | Year |
|---|---|
Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses.
Topics: Amino Acid Metabolism, Inborn Errors; Asian People; Child, Preschool; Developmental Disabilities; Female; Fetus; Humans; Hydroxybutyrates; Infant; Infant, Newborn; Male; Pregnancy; Prenatal Diagnosis; Sequence Deletion; Succinate-Semialdehyde Dehydrogenase | 2015 |
Correlation of blood biomarkers with age informs pathomechanisms in succinic semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Biomarkers; Child; Child, Preschool; Developmental Disabilities; Epilepsy; Female; gamma-Aminobutyric Acid; Humans; Hydroxybutyrates; Male; Succinate-Semialdehyde Dehydrogenase; Synaptic Transmission; Young Adult | 2016 |
Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiency.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Caproates; Child; Child, Preschool; Developmental Disabilities; Evoked Potentials, Visual; Female; Humans; Hydroxybutyrates; Male; Mutation; Succinate-Semialdehyde Dehydrogenase | 2009 |
4-Hydroxybutyric aciduria associated with catheter usage: a diagnostic pitfall in the identification of SSADH deficiency.
Topics: 4-Butyrolactone; Amino Acid Metabolism, Inborn Errors; Catheters; Developmental Disabilities; Female; Humans; Hydroxybutyrates; Infant; Infant, Newborn; Maple Syrup Urine Disease; Succinate-Semialdehyde Dehydrogenase | 2011 |
Monitoring of 4-hydroxybutyric acid levels in body fluids during vigabatrin treatment in succinic semialdehyde dehydrogenase deficiency.
Topics: Aldehyde Oxidoreductases; Child; Developmental Disabilities; Enzyme Inhibitors; Female; Humans; Hydroxybutyrates; Metabolism, Inborn Errors; Succinate-Semialdehyde Dehydrogenase; Treatment Outcome; Vigabatrin | 2003 |
Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: a unique case of gamma-hydroxybutyric aciduria and Williams syndrome.
Topics: Aortic Stenosis, Supravalvular; Developmental Disabilities; Diagnosis, Differential; Disorders of Excessive Somnolence; Failure to Thrive; Female; gamma-Aminobutyric Acid; Humans; Hydroxybutyrates; Infant; Metabolism, Inborn Errors; Succinate-Semialdehyde Dehydrogenase; Williams Syndrome | 2007 |